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Volumn 47, Issue 41, 2008, Pages 7927-7930

Gold(I)-catalyzed alkoxyhalogenation of β-hydroxy-α,α- difluoroynones

Author keywords

Cyclization; Fluorine; Gold; Homogeneous catalysis; Ynones

Indexed keywords


EID: 54749120024     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200802162     Document Type: Article
Times cited : (151)

References (56)
  • 2
    • 4444355871 scopus 로고    scopus 로고
    • H. J. Boehm, D. Banner, S . Bendels, M. Kansy, B . Kuhn, K. Mueller, U. Obst-Sander, M. Stahl, ChemBioChem 2004, 5, 637-643;
    • b) H. J. Boehm, D. Banner, S . Bendels, M. Kansy, B . Kuhn, K. Mueller, U. Obst-Sander, M. Stahl, ChemBioChem 2004, 5, 637-643;
  • 6
    • 0027686845 scopus 로고    scopus 로고
    • T. Taguchi, Y . Kodama, M. Kanazawa, Carbohydr. Res. 1993, 249, 243-252;
    • c) T. Taguchi, Y . Kodama, M. Kanazawa, Carbohydr. Res. 1993, 249, 243-252;
  • 11
    • 2442559990 scopus 로고    scopus 로고
    • S . Di Giuseppe
    • a) A. Arcadi, S . Di Giuseppe, Curr. Org. Chem. 2004, 8, 795-812;
    • (2004) Curr. Org. Chem , vol.8 , pp. 795-812
    • Arcadi, A.1
  • 14
    • 33745446200 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 200-203;
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 200-203
  • 16
    • 33845546747 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 7896-7936;
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 7896-7936
  • 17
    • 34547510627 scopus 로고    scopus 로고
    • e) A. S. K. Hashmi, Chem. Rev. 2007, 107, 3180-3211;
    • (2007) Chem. Rev , vol.107 , pp. 3180-3211
    • Hashmi, A.S.K.1
  • 19
    • 34250824768 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 3410-3449;
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 3410-3449
  • 21
    • 40949091926 scopus 로고    scopus 로고
    • h) H. C. Shen, Tetrahedron 2008, 64, 3885-3903.
    • (2008) Tetrahedron , vol.64 , pp. 3885-3903
    • Shen, H.C.1
  • 23
    • 54749107304 scopus 로고    scopus 로고
    • For examples of capture of vinylgold intermediates with allyl or alkoxyalkyl groups: a I. Nakamura, T. Sato, Y. Yamamoto, Angew. Chem. 2006, 118, 4585-4587;
    • For examples of capture of vinylgold intermediates with allyl or alkoxyalkyl groups: a) I. Nakamura, T. Sato, Y. Yamamoto, Angew. Chem. 2006, 118, 4585-4587;
  • 24
    • 33746309818 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 4473-4475;
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 4473-4475
  • 25
    • 28844458694 scopus 로고    scopus 로고
    • with iminium: b L. Zhang, J. Am. Chem. Soc. 2005, 127, 16804-16805;
    • with iminium: b) L. Zhang, J. Am. Chem. Soc. 2005, 127, 16804-16805;
  • 26
    • 54749138140 scopus 로고    scopus 로고
    • with sulfonyl groups: c I. Nakamura, U. Yamagishi, D. Song, S. Konta, Y. Yamamoto, Angew. Chem. 2007, 119, 2334-2337;
    • with sulfonyl groups: c) I. Nakamura, U. Yamagishi, D. Song, S. Konta, Y. Yamamoto, Angew. Chem. 2007, 119, 2334-2337;
  • 27
    • 34250373793 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 2284-2287;
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 2284-2287
  • 28
    • 33748774422 scopus 로고    scopus 로고
    • with benzyl groups: d P. Dubé, D. Toste, J. Am. Chem. Soc. 2006, 128, 12062-12063;
    • with benzyl groups: d) P. Dubé, D. Toste, J. Am. Chem. Soc. 2006, 128, 12062-12063;
  • 30
    • 35048879619 scopus 로고    scopus 로고
    • with silyl group: f I. Nakamura, S. Takuma, M. Terada, Y. Yamamoto, Org. Lett. 2007, 9, 4081-4083.
    • with silyl group: f) I. Nakamura, S. Takuma, M. Terada, Y. Yamamoto, Org. Lett. 2007, 9, 4081-4083.
  • 31
    • 54749102820 scopus 로고    scopus 로고
    • For examples of capture of vinylgold intermediates with iodine: a S. F. Kirsch, J. T. Binder, B. Crone, A. Duschek, T. T. Haug, C. Liébert, H. Menz, Angew. Chem. 2007, 119, 2360-2363;
    • For examples of capture of vinylgold intermediates with iodine: a) S. F. Kirsch, J. T. Binder, B. Crone, A. Duschek, T. T. Haug, C. Liébert, H. Menz, Angew. Chem. 2007, 119, 2360-2363;
  • 32
    • 34250333483 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 2310-2313;
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 2310-2313
  • 36
    • 0034500269 scopus 로고    scopus 로고
    • with bromine: e S. K. Bhargava, F. Mohr, M. A. Bennett, L. L. Welling, A. C. Willis, Organometallics 2000, 19, 5628-5635;
    • with bromine: e) S. K. Bhargava, F. Mohr, M. A. Bennett, L. L. Welling, A. C. Willis, Organometallics 2000, 19, 5628-5635;
  • 37
    • 54749103227 scopus 로고    scopus 로고
    • with chlorine: f K. Kitadai, M. Takahashi, M. Takeda, S. K. Bhargava, S. H. Privér, M. A. Bennett, Dalton Trans. 2006, 2560-2571;
    • with chlorine: f) K. Kitadai, M. Takahashi, M. Takeda, S. K. Bhargava, S. H. Privér, M. A. Bennett, Dalton Trans. 2006, 2560-2571;
  • 38
    • 6444240772 scopus 로고    scopus 로고
    • C . He
    • g) Z. Shi, C . He, J. Am. Chem. Soc. 2004, 126, 13596-13597.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 13596-13597
    • Shi, Z.1
  • 47
    • 54749105536 scopus 로고    scopus 로고
    • For full experimental details, see the Supporting Information
    • For full experimental details, see the Supporting Information.
  • 49
    • 54749115704 scopus 로고    scopus 로고
    • 3)4] afforded the desired diene 10b in 65% yield.
    • 3)4] afforded the desired diene 10b in 65% yield.
  • 50
    • 54749087221 scopus 로고    scopus 로고
    • Compound 4d was unambiguously characterized by X-ray crystallography.
    • Compound 4d was unambiguously characterized by X-ray crystallography.
  • 52
    • 22944468852 scopus 로고    scopus 로고
    • Y. Hamashima, T . Suzuki, H. Takano, Y. Shimura, M. Sodeoka, J. Am. Chem. Soc. 2005, 127,10164-10165;
    • b) Y. Hamashima, T . Suzuki, H. Takano, Y. Shimura, M. Sodeoka, J. Am. Chem. Soc. 2005, 127,10164-10165;
  • 55
    • 51449084463 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 5993-5996.
    • (2008) Angew. Chem. Int. Ed , vol.47 , pp. 5993-5996
  • 56
    • 54749090145 scopus 로고    scopus 로고
    • 2COPh in 58% yield of isolated product when the reaction was performed at reflux. No reaction occurred at room temperature.
    • 2COPh in 58% yield of isolated product when the reaction was performed at reflux. No reaction occurred at room temperature.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.